Canonical Allele Identifier: PA891845852
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 569470
ClinVar RCV Id: RCV000690102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.His155Tyr
CA402994767
NM_000156.6:c.463C>T